Obesity and its complications are a major health concern in the US and other industrialized nations. Based on the coincident increase in industrial chemical production and the meteoric rise in body weight in recent decades, a mechanistic connection between increased chemical exposure and the obesity 'epidemic'in industrialized nations has been postulated. Bisphenol A (BPA) is a ubiquitous estrogenic endocrine-disrupting chemical used in polycarbonate plastics and epoxy resins commonly found in food and beverage containers, and it is also present in countless other items that we come into contact with daily. BPA has been detected in the urine of 93% of the US population examined with the highest levels detected in the youngest cohort studied, children between 6 and 12 years of age. Data from our laboratory reveal a dose-dependent effect of perinatal BPA exposure on body weight and adiposity in CD-1 mice. However, neither the cause of BPA- associated weight gain nor the pathologic metabolic sequelae of this weight gain are currently elucidated. This proposal seeks funds to test the hypothesis that early life exposure to BPA promotes adult-onset obesity and hallmarks of the Metabolic Syndrome in CD-1 mice by altering energy metabolism in key metabolic tissues. Goals of the proposed research are to 1) determine the internal dose associated with BPA exposure levels that promote adult onset obesity and its complications, 2) determine the relative impact of perinatal vs. combined perinatal and prepubertal BPA exposure on risk for adult-onset obesity, 3) test the hypothesis that early BPA exposure exacerbates the obesitogenic and metabolic impacts of eating a 'western"""""""" diet (i.e., high in saturated fats), 4) test the hypothesis that BPA promotes obesity by altering relevant metabolic pathways in adipose tissue and skeletal muscle, and 5) identify BPA-associated transcriptional and epigenetic changes that underlie altered metabolic rate and/ or promote obesity-associated pathology in BPA-exposed mice. The proposed studies are highly collaborative, involving the integrated efforts of five investigators with distinct but complementary expertise in BPA, obesity and metabolism, diabetes, gene profiling, and epigenetics. Successful completion of the studies in this grant application will provide the first comprehensive and integrated study of how early life BPA exposure promotes adult obesity and its associated complications. These studies will identify the molecular, cell biological, and physiological mechanisms involved in the action of BPA on body weight and in so doing, these studies are likely to contribute to public health policy decisions concerning BPA.

Public Health Relevance

Bisphenol A (BPA), is a ubiquitous chemical used in plastics and commonly found in food and beverage containers. Preliminary studies in our lab have revealed a dose- dependent increase in body weight in rodents exposed to BPA early in life. This proposal will further investigate the potential for BPA to promote obesity in adulthood.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
High Impact Research and Research Infrastructure Programs (RC2)
Project #
1RC2ES018781-01
Application #
7856980
Study Section
Special Emphasis Panel (ZES1-LWJ-J (O1))
Program Officer
Heindel, Jerrold
Project Start
2009-09-30
Project End
2011-07-31
Budget Start
2009-09-30
Budget End
2010-07-31
Support Year
1
Fiscal Year
2009
Total Cost
$800,000
Indirect Cost
Name
Tufts University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
039318308
City
Boston
State
MA
Country
United States
Zip Code
02111
Rubin, Beverly S; Paranjpe, Maneesha; DaFonte, Tracey et al. (2017) Perinatal BPA exposure alters body weight and composition in a dose specific and sex specific manner: The addition of peripubertal exposure exacerbates adverse effects in female mice. Reprod Toxicol 68:130-144
Shimpi, Prajakta C; More, Vijay R; Paranjpe, Maneesha et al. (2017) Hepatic Lipid Accumulation and Nrf2 Expression following Perinatal and Peripubertal Exposure to Bisphenol A in a Mouse Model of Nonalcoholic Liver Disease. Environ Health Perspect 125:087005
Bennett, Grace; Strissel, Katherine J; DeFuria, Jason et al. (2014) Deletion of TNF-like weak inducer of apoptosis (TWEAK) protects mice from adipose and systemic impacts of severe obesity. Obesity (Silver Spring) 22:1485-94
Vandenberg, Laura N; Schaeberle, Cheryl M; Rubin, Beverly S et al. (2013) The male mammary gland: a target for the xenoestrogen bisphenol A. Reprod Toxicol 37:15-23
Vernier, Stephanie; Chiu, Angela; Schober, Joseph et al. (2012) ?-cell metabolic alterations under chronic nutrient overload in rat and human islets. Islets 4:379-92
Ong, Kuok Teong; Mashek, Mara T; Bu, So Young et al. (2011) Adipose triglyceride lipase is a major hepatic lipase that regulates triacylglycerol turnover and fatty acid signaling and partitioning. Hepatology 53:116-26
Rubin, Beverly S (2011) Bisphenol A: an endocrine disruptor with widespread exposure and multiple effects. J Steroid Biochem Mol Biol 127:27-34
Greenberg, Andrew S; Coleman, Rosalind A; Kraemer, Fredric B et al. (2011) The role of lipid droplets in metabolic disease in rodents and humans. J Clin Invest 121:2102-10